EP2298778A4 - Dérivé d imidazothiazole ayant une structure cyclique de 4,7-diazaspiroý2.5¨octane - Google Patents
Dérivé d imidazothiazole ayant une structure cyclique de 4,7-diazaspiroý2.5¨octaneInfo
- Publication number
- EP2298778A4 EP2298778A4 EP09762499A EP09762499A EP2298778A4 EP 2298778 A4 EP2298778 A4 EP 2298778A4 EP 09762499 A EP09762499 A EP 09762499A EP 09762499 A EP09762499 A EP 09762499A EP 2298778 A4 EP2298778 A4 EP 2298778A4
- Authority
- EP
- European Patent Office
- Prior art keywords
- imidazothiazole
- diazaspiro
- derivate
- cyclic structure
- cyclic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008154036 | 2008-06-12 | ||
| PCT/JP2009/060575 WO2009151069A1 (fr) | 2008-06-12 | 2009-06-10 | Dérivé d’imidazothiazole ayant une structure cyclique de 4,7-diazaspiro[2.5]octane |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP2298778A1 EP2298778A1 (fr) | 2011-03-23 |
| EP2298778A4 true EP2298778A4 (fr) | 2011-10-05 |
Family
ID=41416775
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP09762499A Withdrawn EP2298778A4 (fr) | 2008-06-12 | 2009-06-10 | Dérivé d imidazothiazole ayant une structure cyclique de 4,7-diazaspiroý2.5¨octane |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP2298778A4 (fr) |
| JP (1) | JPWO2009151069A1 (fr) |
| TW (1) | TW201002724A (fr) |
| WO (1) | WO2009151069A1 (fr) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT2380892E (pt) * | 2009-01-16 | 2014-06-09 | Daiichi Sankyo Co Ltd | Derivado de imidazotiazole compreendendo uma estrutura de anel prolina |
| KR20120099462A (ko) | 2009-11-12 | 2012-09-10 | 더 리젠츠 오브 더 유니버시티 오브 미시건 | 스피로-옥신돌 mdm2 길항제 |
| AU2011326395B2 (en) | 2010-11-12 | 2016-01-07 | Ascenta Licensing Corporation | Spiro-oxindole MDM2 antagonists |
| US8629141B2 (en) | 2011-05-11 | 2014-01-14 | The Regents Of The University Of Michigan | Spiro-oxindole MDM2 antagonists |
| TW201429969A (zh) | 2012-12-20 | 2014-08-01 | Merck Sharp & Dohme | 作爲hdm2抑制劑之經取代咪唑吡啶 |
| US20170216286A1 (en) | 2014-01-28 | 2017-08-03 | Mayo Foundation For Medical Education And Research | Killing senescent cells and treating senescence-associated conditions using a src inhibitor and a flavonoid |
| US10328058B2 (en) | 2014-01-28 | 2019-06-25 | Mayo Foundation For Medical Education And Research | Treating atherosclerosis by removing senescent foam cell macrophages from atherosclerotic plaques |
| AU2015211021B2 (en) | 2014-01-28 | 2020-07-02 | Buck Institute For Research On Aging | Methods and compositions for killing senescent cells and for treating senescence-associated diseases and disorders |
| CN105111155B (zh) * | 2015-08-31 | 2018-12-14 | 武汉工程大学 | 一种4,7-二氮杂螺[2.5]辛烷-7-甲酸叔丁酯的合成方法 |
| WO2017176958A1 (fr) | 2016-04-06 | 2017-10-12 | The Regents Of The University Of Michigan | Intermédiaires monofonctionnels pour la dégradation d'une protéine cible dépendante du ligand |
| AU2017246452C1 (en) | 2016-04-06 | 2021-06-03 | The Regents Of The University Of Michigan | MDM2 protein degraders |
| EP3458101B1 (fr) | 2016-05-20 | 2020-12-30 | H. Hoffnabb-La Roche Ag | Conjugués anticorps-protac et procédés d'utilisation |
| CN108530375B (zh) * | 2018-05-29 | 2020-04-21 | 南京药石科技股份有限公司 | 4-氧杂-7-氮杂螺[2.5]辛烷或其盐的中间体及制备方法 |
| CN111943894A (zh) * | 2019-05-17 | 2020-11-17 | 南京爱德程医药科技有限公司 | 一种4,7-二氮杂螺[2.5]辛烷类化合物的合成方法 |
| CN111943893B (zh) * | 2019-05-17 | 2024-07-26 | 南京爱德程医药科技有限公司 | 4,7-二氮杂螺[2,5]辛烷类化合物的合成方法 |
| WO2023056069A1 (fr) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Conjugués agent de dégradation-anticorps et leurs procédés d'utilisation |
| WO2023165523A1 (fr) * | 2022-03-01 | 2023-09-07 | 上海璎黎药业有限公司 | Dérivé méthoxy substitué par un cycle aromatique et son utilisation |
| WO2024240858A1 (fr) | 2023-05-23 | 2024-11-28 | Valerio Therapeutics | Molécules protac dirigées contre un système de réparation de dommages à l'adn et leurs utilisations |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1167369A1 (fr) * | 1999-04-06 | 2002-01-02 | Yamanouchi Pharmaceutical Co. Ltd. | Nouveaux derives de thiazolobenzimidazole |
| US6696441B1 (en) * | 2000-08-11 | 2004-02-24 | The Regents Of The University Of California | Inhibition of p53-induced stress response |
| EP1486501A1 (fr) * | 2002-03-20 | 2004-12-15 | Yamanouchi Pharmaceutical Co. Ltd. | Derive de thiazolobenzimidazole substitue par aminomethyle |
| WO2010082612A1 (fr) * | 2009-01-16 | 2010-07-22 | 第一三共株式会社 | Dérivé d'imidazothiazole comprenant une structure de noyau proline |
Family Cites Families (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US526916A (en) | 1894-10-02 | Milking-stool | ||
| WO1997048706A1 (fr) | 1996-06-18 | 1997-12-24 | Warner-Lambert Company | Pyrrolo(1,2-a)pyrazine 1,4-diones servant d'inhibiteurs des serines proteases |
| US6238921B1 (en) | 1998-03-26 | 2001-05-29 | Isis Pharmaceuticals, Inc. | Antisense oligonucleotide modulation of human mdm2 expression |
| JP2000072743A (ja) | 1998-08-31 | 2000-03-07 | Japan Science & Technology Corp | アルケンのアジリジン化法 |
| GB9819860D0 (en) | 1998-09-12 | 1998-11-04 | Zeneca Ltd | Chemical compounds |
| US6979551B2 (en) | 2000-04-03 | 2005-12-27 | Rigel Pharmaceuticals, Inc. | Assays for identifying ubiquitin agents and for identifying agents that modify the activity of ubiquitin agents |
| US6740495B1 (en) | 2000-04-03 | 2004-05-25 | Rigel Pharmaceuticals, Inc. | Ubiquitin ligase assay |
| PT1443937E (pt) | 2001-11-13 | 2008-09-23 | Ortho Mcneil Janssen Pharm | 1,4-benzodiazepinas substituídas e as suas utilizações para o tratamento de cancro |
| BR0215156A (pt) | 2001-12-18 | 2004-10-19 | Hoffmann La Roche | Cis-imidazolinas como inibidores de mdm 2 |
| BR0215157A (pt) | 2001-12-18 | 2004-10-19 | Hoffmann La Roche | Cis-2,4,5-trifenil-imidazolinas e seu uso no tratamento de tumores |
| WO2003095625A2 (fr) | 2002-05-13 | 2003-11-20 | 3-Dimensional Pharmaceuticals, Inc. | Procede de cytoprotection par inhibition de mdm2 et de hdm2 |
| GB0215650D0 (en) * | 2002-07-05 | 2002-08-14 | Cyclacel Ltd | Bisarylsufonamide compounds |
| US20040197893A1 (en) | 2002-10-16 | 2004-10-07 | Carsten Schubert | HDM2-inhibitor complexes and uses thereof |
| GB0225548D0 (en) | 2002-11-01 | 2002-12-11 | Glaxo Group Ltd | Compounds |
| US6916833B2 (en) | 2003-03-13 | 2005-07-12 | Hoffmann-La Roche Inc. | Substituted piperidines |
| WO2004094407A1 (fr) | 2003-04-21 | 2004-11-04 | Daiichi Pharmaceutical Co. Ltd. | Derive heterocyclique a cinq chainons |
| US20040213264A1 (en) | 2003-04-25 | 2004-10-28 | Nortel Networks Limited | Service class and destination dominance traffic management |
| UA82230C2 (en) | 2003-04-25 | 2008-03-25 | Орто-Макнейл Фармасьютикел, Инк. | Substituted 1,4-diazepines and uses thereof |
| GB0309637D0 (en) * | 2003-04-28 | 2003-06-04 | Cancer Rec Tech Ltd | Pyrazole compounds |
| US7425638B2 (en) | 2003-06-17 | 2008-09-16 | Hoffmann-La Roche Inc. | Cis-imidazolines |
| CN100562316C (zh) | 2003-06-17 | 2009-11-25 | 霍夫曼-拉罗奇有限公司 | 作为mdm2抑制剂的顺式咪唑啉 |
| AU2004254187A1 (en) | 2003-06-17 | 2005-01-13 | F. Hoffmann-La Roche Ag | Cis-2,4,5-triaryl-imidazolines |
| US7132421B2 (en) | 2003-06-17 | 2006-11-07 | Hoffmann-La Roche Inc. | CIS-imidazoles |
| GB0324498D0 (en) | 2003-07-21 | 2003-11-26 | Aventis Pharma Inc | Heterocyclic compounds as P2X7 ion channel blockers |
| JP2005075754A (ja) | 2003-08-29 | 2005-03-24 | Mitsui Chemicals Inc | トランス−1,2−ビス(3,5−ジメチルフェニル)−1,2−エタンジアミンの光学分割方法 |
| JP2005306839A (ja) * | 2003-08-29 | 2005-11-04 | Takeda Chem Ind Ltd | 二環性ピペラジン化合物およびその用途 |
| BRPI0511328A (pt) | 2004-05-18 | 2007-12-04 | Hoffmann La Roche | cis-imidazolinas |
| US7893278B2 (en) | 2004-06-17 | 2011-02-22 | Hoffman-La Roche Inc. | CIS-imidazolines |
| GB0419481D0 (en) | 2004-09-02 | 2004-10-06 | Cancer Rec Tech Ltd | Isoindolin-1-one derivatives |
| KR100944301B1 (ko) | 2005-02-22 | 2010-02-24 | 더 리젠츠 오브 더 유니버시티 오브 미시간 | Mdm2의 소분자 억제제 및 이의 용도 |
| JP4955646B2 (ja) | 2005-03-16 | 2012-06-20 | エフ.ホフマン−ラ ロシュ アーゲー | シス−2,4,5−トリアリール−イミダゾリン及びそれらの抗癌薬としての使用 |
| US8211919B2 (en) | 2005-09-02 | 2012-07-03 | Astellas Pharma Inc. | Amide derivatives as rock inhibitors |
| CN101316823B (zh) | 2005-12-01 | 2013-05-22 | 霍夫曼-拉罗奇有限公司 | 用作抗癌剂的作为p53和MDM2蛋白之间相互作用的抑制剂的2,4,5-三苯基咪唑啉衍生物 |
| SG174107A1 (en) | 2006-08-30 | 2011-09-29 | Univ Michigan | New small molecule inhibitors of mdm2 and the uses thereof |
| AU2007332493A1 (en) * | 2006-12-14 | 2008-06-19 | Daiichi Sankyo Company, Limited | Imidazothiazole derivatives |
| PL2134720T3 (pl) | 2007-03-29 | 2011-04-29 | Novartis Ag | Heterocykliczne spiro-związki |
-
2009
- 2009-06-10 WO PCT/JP2009/060575 patent/WO2009151069A1/fr not_active Ceased
- 2009-06-10 EP EP09762499A patent/EP2298778A4/fr not_active Withdrawn
- 2009-06-10 JP JP2010516864A patent/JPWO2009151069A1/ja active Pending
- 2009-06-11 TW TW098119478A patent/TW201002724A/zh unknown
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1167369A1 (fr) * | 1999-04-06 | 2002-01-02 | Yamanouchi Pharmaceutical Co. Ltd. | Nouveaux derives de thiazolobenzimidazole |
| US6696441B1 (en) * | 2000-08-11 | 2004-02-24 | The Regents Of The University Of California | Inhibition of p53-induced stress response |
| EP1486501A1 (fr) * | 2002-03-20 | 2004-12-15 | Yamanouchi Pharmaceutical Co. Ltd. | Derive de thiazolobenzimidazole substitue par aminomethyle |
| WO2010082612A1 (fr) * | 2009-01-16 | 2010-07-22 | 第一三共株式会社 | Dérivé d'imidazothiazole comprenant une structure de noyau proline |
Non-Patent Citations (1)
| Title |
|---|
| See also references of WO2009151069A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| TW201002724A (en) | 2010-01-16 |
| EP2298778A1 (fr) | 2011-03-23 |
| JPWO2009151069A1 (ja) | 2011-11-17 |
| WO2009151069A1 (fr) | 2009-12-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| 17P | Request for examination filed |
Effective date: 20101223 |
|
| AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK TR |
|
| AX | Request for extension of the european patent |
Extension state: AL BA RS |
|
| DAX | Request for extension of the european patent (deleted) | ||
| A4 | Supplementary search report drawn up and despatched |
Effective date: 20110906 |
|
| RIC1 | Information provided on ipc code assigned before grant |
Ipc: A61P 43/00 20060101ALI20110831BHEP Ipc: A61P 35/00 20060101ALI20110831BHEP Ipc: A61K 31/496 20060101ALI20110831BHEP Ipc: C07D 513/04 20060101AFI20110831BHEP |
|
| GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
| INTG | Intention to grant announced |
Effective date: 20130610 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
| 18D | Application deemed to be withdrawn |
Effective date: 20131022 |